Matthew Hurles

Hurles was privately educated at Hampton School^[1] and the University of Oxford where he was awarded a Bachelor of Arts degree in Biochemistry. He completed his PhD in 1999 on the genetics of the Y chromosome at the University of Leicester supervised by Mark Jobling^[3][8][9]

Hurles research investigates the causes and consequences of new mutations as DNA is passed from one generation to the next.^[4] He is best known for his work on characterizing the extent and impact of structural variation in the human genome and on deciphering the genetic architecture of severe neurodevelopmental disorders.^[4]

Hurles group has used large-scale genomic studies to highlight the predominant role that new mutations of many different types play in causing diverse developmental disorders and has led to the discovery of tens of previously unrecognised genetic diseases.^{[4][10][11][12]}

Hurles was elected a Fellow of the Royal Society (FRS) in 2019.^[1][4] He is also a Fellow of the Academy of Medical Sciences (FMedSci) and was awarded the Crick Medal and Lecture in 2013.^[4]